{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82587",
      "recalling_firm": "DePuy Spine, Inc.",
      "address_1": "325 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-5199",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution. Foreign distribution to Austria, Switzerland, and United Kingdom.",
      "recall_number": "Z-1226-2019",
      "product_description": "Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x27 (197811027L), 9x23 (US197809023L), 9x27 (US197809027L)",
      "product_quantity": "3166 total",
      "reason_for_recall": "A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.",
      "recall_initiation_date": "20190408",
      "center_classification_date": "20190426",
      "termination_date": "20230112",
      "report_date": "20190508",
      "code_info": "All lots"
    }
  ]
}